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Organism with a recessive genetic allele that does not display the recessive trait
A hereditary carrier (genetic carrier or just carrier) is a person or other organism that has inherited a recessive allele for a genetic trait or mutation
Hereditary_carrier
Genetic condition involving iron buildup
this autosomal recessive condition, their parents have acted as hereditary carriers, possessing one copy of the mutated gene but not manifesting any
Hereditary_haemochromatosis
Hereditary blood disorder causing anemia
distribution of Plasmodium falciparum malaria, and it is likely that a hereditary carrier of a gene for beta-thalassemia has some protection from severe malaria
Beta_thalassemia
Health problem from genome abnormalities
genes are generally sufficient to prevent symptoms in carriers. On the other hand, hereditary defects in structural proteins (such as osteogenesis imperfecta
Genetic_disorder
Genetic disorder causing red blood cells to be spherical
Hereditary spherocytosis (HS) is a congenital hemolytic disorder wherein a genetic mutation coding for a structural membrane protein phenotype causes the
Hereditary_spherocytosis
First Nations people of British Columbia, Canada
branch of the Dakelh or Carrier people, and in combination with the Babine people have been referred to as the Western Carrier.[citation needed] They speak
Wetʼsuwetʼen
Dog breed
Basrur, PK (1986). "Mode of inheritance of Samoyed hereditary glomerulopathy: an animal model for hereditary nephritis in humans". The Journal of Laboratory
Samoyed_dog
Inherited condition raising colon cancer risk
Hereditary nonpolyposis colorectal cancer (HNPCC) is a hereditary predisposition to colon cancer. HNPCC is synonymous with Lynch syndrome, an autosomal
Hereditary nonpolyposis colorectal cancer
Hereditary_nonpolyposis_colorectal_cancer
Disorder resulting in severe swelling
However, hereditary angioedema with normal C1 inhibitor levels (Type 3 disease) has incomplete penetrance, and men may be asymptomatic carriers despite
Hereditary_angioedema
Inherited genetic condition that predisposes a person to cancer
A hereditary cancer syndrome (familial/family cancer syndrome, inherited cancer syndrome, cancer predisposition syndrome, cancer syndrome) is a genetic
Hereditary_cancer_syndrome
Topics referred to by the same term
small intestine in which the fructose carrier in enterocytes is deficient Hereditary fructose intolerance, a hereditary condition caused by a deficiency of
Fructose_intolerance
Sequence of DNA that determines traits in an organism
in which he postulated that different characters have individual hereditary carriers and that inheritance of specific traits in organisms comes in particles
Gene
Indigenous people in British Columbia, Canada
The Dakelh (pronounced ['takʰɛɬ]) or Carrier are a First Nations Indigenous people living a large portion of the Central Interior of British Columbia
Dakelh
Genetic haematological condition
Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an abnormally large number of the person's red blood cells
Hereditary_elliptocytosis
Dutch botanist (1848–1935)
of 1868, he postulated that different characters have different hereditary carriers. He specifically postulated that inheritance of specific traits in
Hugo_de_Vries
Mitochondrially inherited degeneration of retinal nerve cells
Leber's hereditary optic neuropathy (LHON) is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells
Leber's hereditary optic neuropathy
Leber's_hereditary_optic_neuropathy
in which he postulated that different characters have different hereditary carriers, based on a modified version of Charles Darwin's theory of Pangenesis
List_of_Dutch_discoveries
Medical condition
Hereditary breast–ovarian cancer syndromes (HBOC) are cancer syndromes that produce higher than normal levels of breast cancer, ovarian cancer and additional
Hereditary breast–ovarian cancer syndrome
Hereditary_breast–ovarian_cancer_syndrome
Inflammatory muscle disease in older adults
is often confused with an entirely different class of diseases, called hereditary inclusion body myopathies (hIBM). The "M" in hIBM is an abbreviation for
Inclusion_body_myositis
Metabolic disorders in which porphyrins build up in the body
porphyria (VP), aminolevulinic acid dehydratase deficiency porphyria (ALAD), hereditary coproporphyria (HCP), and porphyria cutanea tarda. Treatment depends on
Porphyria
Passing of traits to offspring from the species' parents or ancestor
genes are generally sufficient to prevent symptoms in carriers. On the other hand, hereditary defects in structural proteins (such as osteogenesis imperfecta
Heredity
Condition of elevated methemoglobin in the blood
brown. This results in the skin of white patients gaining a bluish hue. Hereditary met-Hb is caused by a recessive gene. If only one parent has this gene
Methemoglobinemia
Genetic disease in Quarter Horses, Appaloosas, and Paint Horses
Hereditary equine regional dermal asthenia (HERDA), also known as hyperelastosis cutis (HC), is an inherited autosomal recessive connective tissue disorder
Hereditary equine regional dermal asthenia
Hereditary_equine_regional_dermal_asthenia
Medical condition of the dog breed
Samoyed hereditary glomerulopathy (SHG) is a hereditary, X-linked, noninflammatory disease of the renal glomeruli, occurring in the Samoyed breed of dog
Samoyed hereditary glomerulopathy
Samoyed_hereditary_glomerulopathy
Medical condition
a decade earlier than non-hereditary cases. Asymptomatic screening is invasive and may be recommended only to BRCA2 carriers who also have a family history
BRCA_mutation
Keyoh is a term in the Dakelh (Carrier) language meaning territory, village, or trapline. It refers to a traditional Indigenous land governance system
Keyoh
Autosomal dominant cancer syndrome
Li–Fraumeni syndrome (LFS) is a rare, autosomal dominant, hereditary disorder that predisposes carriers to cancer development. It was named after two American
Li–Fraumeni_syndrome
American clinical genetic testing company
company introduced the Anora miscarriage (POC) test. Natera's advanced carrier screening test, Horizon, launched in 2012. The following year, 2013, Natera
Natera
Abnormal accumulation of iron in the body
formation via the Fenton reaction. Iron overload is often primary (i.e., hereditary haemochromatosis, aceruloplasminemia) but may also be secondary to other
Iron_overload
Medical condition
syndrome once also had the label hereditary nephritis, but this is misleading as there are many other causes of hereditary kidney disease and 'nephritis'
Alport_syndrome
Genetic disorder in European royalty
Prince Alfred, Duke of Saxe-Coburg and Gotha (1844–1900) Issue: Alfred, Hereditary Prince of Saxe-Coburg and Gotha, Marie, Queen of Romania, Grand Duchess
Haemophilia in European royalty
Haemophilia_in_European_royalty
Clouding of the transparent cornea of the eye
Corneal dystrophy is a group of rare hereditary disorders characterised by bilateral abnormal deposition of substances in the transparent front part of
Corneal_dystrophy
Medical condition
symptoms are male, due to the X-linked pattern of inheritance, but female carriers can be affected due to unfavorable lyonization or skewed X-inactivation
Glucose-6-phosphate dehydrogenase deficiency
Glucose-6-phosphate_dehydrogenase_deficiency
Most common genetic condition leading to color blindness
colorblind. Colorblind females can only produce colorblind males. Because carrier females often have a colorblind father, colorblind males often will have
Congenital red–green color blindness
Congenital_red–green_color_blindness
King of the United Kingdom since 2022
the Commonwealth after the Queen. The head is chosen and therefore not hereditary. In March 2019, at the request of the British government, Charles and
Charles_III
Medical condition
Lawrence Day in 1949, FD is one example of a group of disorders known as hereditary sensory and autonomic neuropathies (HSANs). All HSANs are characterized
Familial_dysautonomia
American family known for blue skin
who had married and settled near Hazard, Kentucky about 1820, were both carriers of the rare recessive methemoglobinemia (met-H) gene. As a result, four
Blue_Fugates
Mitochondrial protein involved in iron–sulfur cluster biosynthesis
with a mitochondrial myopathy called hereditary myopathy with lactic acidosis (HML). It is also known as hereditary myopathy with exercise intolerance,
ISCU
Medical condition
with hereditary fructose intolerance, a potentially fatal condition in which the liver enzymes that break up fructose are deficient. Hereditary fructose
Fructose_malabsorption
Country in Southeast Asia
Agong. The King is elected to a five-year term by and from among the nine hereditary rulers of the Malay states. The other four states, which have titular
Malaysia
Country primarily in Western Europe
feudal society. As central authority faltered, local nobility secured hereditary rights to their titles and lands, creating a system where the king's authority
France
Brief history of Constantinople from 330 to 1453
authorities. Artisans were bound to these workshops for life, and this duty was hereditary. In addition, a significant portion of the workshop workers were slaves
History_of_Constantinople
Mammalian protein found in Homo sapiens
Anion exchange protein 1 (AE1), also known as solute carrier family 4 member 1, is a protein that is encoded by the SLC4A1 gene in humans. Anion exchange
Anion_exchange_protein_1
Country in East Asia
Japan Airlines, the flag carrier of Japan
Japan
Enlargement of the heart muscle
left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations". Journal of the American College
Hypertrophic_cardiomyopathy
Form of treatment for genetic disorders and other illnesses
hypercholesterolemia. Inotersen received FDA approval for the treatment of hereditary transthyretin-mediated amyloidosis in October 2018. The application for
Antisense_therapy
Medical condition
Congenital hereditary corneal dystrophy (CHED) is a form of corneal endothelial dystrophy that presents at birth. CHED was previously subclassified into
Congenital hereditary endothelial dystrophy
Congenital_hereditary_endothelial_dystrophy
First Nations government in Canada
(French: conseil de bande) chaired by an elected chief, and sometimes also a hereditary chief. Membership is determined either through the Indian Register maintained
Band_government
Former empire (c. 1299–1922)
destruction of the Emirate of Diriyah in 1818. The suzerainty of Serbia as a hereditary monarchy under its own dynasty was acknowledged de jure in 1830. In 1821
Ottoman_Empire
Medical condition
Hereditary folate malabsorption (HFM) is a rare autosomal recessive disorder caused by loss-of-function mutations in the proton-coupled folate transporter
Hereditary folate malabsorption
Hereditary_folate_malabsorption
recessive disorders is focused on making it less likely that two carriers for the same hereditary disease will have children together. Some genetic disorders
Prevention of autosomal recessive disorders
Prevention_of_autosomal_recessive_disorders
Group of genetic connective tissues disorders
with a patient and doctor who have EDS. Ehlers–Danlos–like syndromes are hereditary in Himalayan cats, some domestic shorthair cats, and certain breeds of
Ehlers–Danlos_syndrome
Autosomal recessive conditions that affect ethnic Jews more frequently
groups tend to have different rates of hereditary diseases, with some being more common, and some less common. Hereditary diseases, particularly hemophilia
Medical_genetics_of_Jews
Breed of herding dog
most common health problems are deafness and progressive blindness (both hereditary conditions) and accidental injury. Thomas Simpson Hall, pastoralist and
Australian_Cattle_Dog
Condition in which damaged skeletal muscle breaks down rapidly
simultaneously in one person. Some have an underlying muscle condition, usually hereditary, that makes them more prone to rhabdomyolysis. Recurrent or episodic rhabdomyolysis
Rhabdomyolysis
Haem or Heme carrier protein 1 (HCP1) is a protein found in the small intestine that plays a role in the absorption of dietary heme, a form of iron that
Haem_carrier_protein_1
Genetic skeletal disease
increased the intra-community incidence of certain hereditary disorders, including Van Buchem's; of carrier status for the autosomal recessive conditions among
Van_Buchem_disease
Medical condition
H. (June 2015). "Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers". Journal of Medical
Hereditary diffuse gastric cancer
Hereditary_diffuse_gastric_cancer
Country in West Asia
semi-presidential state under a semi-constitutional monarchy made up of seven hereditary tribal monarchy-styled political units called Sheikhdoms. It is governed
United_Arab_Emirates
Mother of Queen Victoria (1786–1861)
Duchess herself to be a carrier of haemophilia, since haemophilia is X-linked, meaning that her mother would have been a carrier, if haemophilia was not
Princess Victoria of Saxe-Coburg-Saalfeld
Princess_Victoria_of_Saxe-Coburg-Saalfeld
Rare congenital neuromuscular disorder
disorder: the parents may be carriers and not personally affected. SMA seems to appear de novo (i.e., without any hereditary causes) in around 2–4% of cases
Spinal_muscular_atrophy
Evolutionary theory
of the photosystems is lost from the plastid, the intermediate electron carriers may lose or gain too many electrons, signalling the need for repair of
Symbiogenesis
Condition involving an enlarged, ineffective heart
common cause of dilated cardiomyopathy. As opposed to these hereditary forms, non-hereditary DCM used to be common in the overall cat population before
Dilated_cardiomyopathy
Medical condition
Hereditary cystatin C amyloid angiopathy (HCCAA) is a rare, fatal type of hereditary cerebral amyloid angiopathy found almost exclusively in Iceland. A
Hereditary cystatin C amyloid angiopathy
Hereditary_cystatin_C_amyloid_angiopathy
beautiful long blonde hair turned out to be a wig which concealed the hereditary flat cranium. Although a legitimate business success, she was consumed
List_of_Dick_Tracy_characters
Dog breed
dysplasia, hereditary eye disease, heart/cardiac abnormalities (specifically pulmonary stenosis), hereditary patellar luxation, hereditary exercise-induced
Boykin_Spaniel
Inherited neurodegenerative disorder
discovered in 1993 by an international collaborative effort led by the Hereditary Disease Foundation. Research and support organizations began forming in
Huntington's_disease
of Viktor Brack (1904-1948). As part of the "Law for the Prevention of Hereditary Diseases," people were often subjected to radiation castration during
History of radiation protection
History_of_radiation_protection
Oxygen carrier protein in the human fetus
foetal haemoglobin (also hemoglobin F, HbF, or α2γ2) is the main oxygen carrier protein in the human fetus. Hemoglobin F is found in fetal red blood cells
Fetal_hemoglobin
Hereditary dog disease
epileptoid cramping syndrome (CECS), previously known as Spike's disease, is a hereditary dog disease initially found in Border Terriers and has since been documented
Canine epileptoid cramping syndrome
Canine_epileptoid_cramping_syndrome
Breed of domestic cat
between the two in terms of body language, vocalisations, and feline hereditary diseases. Research on the body language and vocalisation of the two sister
Neva_Masquerade
Breed of cat
of cat, the Traditional Persian, which has a more pronounced muzzle. Hereditary polycystic kidney disease (PKD) is prevalent in the breed, affecting almost
Persian_cat
British peer and UK Independence Party politician
of Lords in 1999, when the House of Lords Act 1999 removed all but 92 hereditary peers, and he was not one of the 92 who were elected to keep their seats
Alexander Fermor-Hesketh, 3rd Baron Hesketh
Alexander_Fermor-Hesketh,_3rd_Baron_Hesketh
Medical blood test to measure transferrin
indirectly measures transferrin since transferrin is the most dynamic carrier. If TIBC values are known, the transferrin concentration can be estimated
Total_iron-binding_capacity
Country in Southeastern and Central Europe
consolidation of Serbia's autonomy, culminating in the recognition of hereditary rule for the Serbian princes in 1830 and 1833 and the adoption of the
Serbia
Country in Southeast Asia
in which a single party cannot easily gain a majority in the House. A hereditary monarch serves as head of state. The current King of Thailand is Vajiralongkorn
Thailand
Joints that stretch farther than normal
other conditions. These include ADHD, autism, dyspraxia, fibromyalgia, hereditary connective tissue disorders, mitral valve prolapse, and anxiety disorders
Hypermobility_(joints)
Medical condition
accumulation in the brain. Children of affected individuals are obligate carriers for aceruloplasminemia. If the CP mutations has been identified in a related
Aceruloplasminemia
Degenerative brain disease caused by prions
disease. There are three main categories of CJD disease: sporadic CJD, hereditary CJD, and acquired CJD, with variant CJD being in the acquired group along
Variant Creutzfeldt–Jakob disease
Variant_Creutzfeldt–Jakob_disease
Country in Southeastern Europe
and in later years the Ottoman Empire enacted a policy of creation of hereditary estates, effectively turning the rural Greek populations into serfs, while
Greece
Breed of cat
through backcrossing. The gene responsible is recessive, meaning that two carrier Bengals can produce long-haired offspring. Genetic testing, including a
Bengal_cat
Breed of domestic cat
maintain a healthy cat breed by controlling inbreeding and the spread of hereditary diseases, and regulating the well-being of the cats. Unregistered cats
Siberian_cat
Queen of Spain from 1906 to 1931
according to the due tenor of the law of England, forfeits for ever all hereditary rights of succession to the Crown and Government of Great Britain… The
Victoria Eugenie of Battenberg
Victoria_Eugenie_of_Battenberg
Cancerous tumor of the developing eye
have the eye removed. Almost half of children with retinoblastoma have a hereditary genetic defect associated with it. In other cases, retinoblastoma is caused
Retinoblastoma
British filmmaker (born 1960)
office of Lord Great Chamberlain is a Cholmondeley inheritance. This hereditary honour came into the Cholmondeley family through the marriage of the first
David Cholmondeley, 7th Marquess of Cholmondeley
David_Cholmondeley,_7th_Marquess_of_Cholmondeley
Duke of Florence from 1532 to 1537
from 1530 to his death in 1537. The first Medici to rule Florence as a hereditary monarch, Alessandro was also the last Medici from the senior line of the
Alessandro de' Medici, Duke of Florence
Alessandro_de'_Medici,_Duke_of_Florence
Similar to membership in the nobility, the rank of chief was mostly hereditary in certain families, but could be revoked. The extremely rainy region
History of the Coast Salish peoples
History_of_the_Coast_Salish_peoples
First-run airings of the ITV medical dramedy
collapses during the job, Sam is examined by Martin for symptoms of the hereditary Huntington's disease, causing Joe to worry that he also might also have
List_of_Doc_Martin_episodes
Country in Central Europe
Therefore, most of the territory that later became Slovenia emerged as a hereditary land of the Habsburg monarchy. As with the other component parts of the
Slovenia
Group of carrier proteins which bind with vitamin B12 in the blood
Group of carrier proteins which bind with vitamin B12 in the blood
Transcobalamin
History of Native American people
as hostage a chief named Chief Tuskaloosa, demanding of him carriers and women. The carriers he got at once. The women, Tuscaloosa said, would be waiting
History_of_the_Choctaw
Eye disease involving splitting of the retina
very common and almost exclusively involve the peripheral retina and hereditary forms which are rare and involve the central retina and sometimes the
Retinoschisis
1882 play written by Henrik Ibsen
he thought – as Oswald is told by his doctor in Ghosts – that it was a hereditary disease passed by father to son. It's much more probable, given that he
Ghosts_(play)
British graphic designer
6th Earl of Munster. From then until the Government's expulsion of the hereditary peers in 1999, as part of the House of Lords Act 1999, he was a regular
Anthony FitzClarence, 7th Earl of Munster
Anthony_FitzClarence,_7th_Earl_of_Munster
Country in West Asia
Islam. Article 4 of the Kuwait constitution stipulates that Kuwait is a hereditary emirate whose emir must be an heir of Mubarak Al-Sabah. Mubarak had four
Kuwait
Overview of the history of Peru, 1821–1842
matters, it put an end to certain remnants of colonial life, namely: hereditary employments, estates, ties and privileges. Torture and infamous punishments
History_of_Peru_(1821–1842)
Island in French Polynesia
of the Pōmare, local chiefs won back some of their power and took the hereditary title of Tavana (from the English word "governor"). The missionaries also
Tahiti
Rare neurodegenerative disease
linked to a family history of ALS; such cases are known as familial ALS or hereditary ALS. Mutations in the C9orf72 gene are the most common known genetic cause
ALS
2014 space trading and exploration simulator
distances. Players can also acquire capital ships: Drake-Class Carrier and the Javelin-Class Carrier. The Drake is like a mobile base for players with billions
Elite_Dangerous
French executioner (1739–1806)
judicial offices under the Ancien Régime, the office of executioner was hereditary in practice and remained within a small number of interrelated families
Charles-Henri_Sanson
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HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
HEREDITARY CARRIER
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